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Clinical and neuroanatomical characterization of the semantic behavioral variant of frontotemporal dementia in a multicenter Italian cohort.
- Published in:
- Journal of Neurology, 2024, v. 271, n. 7, p. 4203, doi. 10.1007/s00415-024-12338-9
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- Publication type:
- Article
Modeling pathological spread through the structural connectome in the FTLD spectrum.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.076398
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- Publication type:
- Article
Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates.
- Published in:
- 2023
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- Publication type:
- Case Study
24-Hydroxycholesterol Induces Tau Proteasome-Dependent Degradation via the SIRT1/PGC1α/Nrf2 Pathway: A Potential Mechanism to Counteract Alzheimer's Disease.
- Published in:
- Antioxidants, 2023, v. 12, n. 3, p. 631, doi. 10.3390/antiox12030631
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- Publication type:
- Article
Semantic and right temporal variant of FTD: Next generation sequencing genetic analysis on a single-center cohort.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.1085406
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- Publication type:
- Article
Significance and clinical suggestions for the somatosensory evoked potentials increased in amplitude revealed by a large sample of neurological patients.
- Published in:
- 2022
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- Publication type:
- journal article
MAPT Q336H mutation: Intrafamilial phenotypic heterogeneity in a new Italian family.
- Published in:
- European Journal of Neurology, 2022, v. 29, n. 5, p. 1529, doi. 10.1111/ene.15250
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- Publication type:
- Article
PMCA-Based Detection of Prions in the Olfactory Mucosa of Patients With Sporadic Creutzfeldt–Jakob Disease.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.848991
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- Publication type:
- Article
Brain MRI signatures of atrophy in genetic frontotemporal lobar degeneration.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, p. 1, doi. 10.1002/alz.053774
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- Publication type:
- Article
Converging longitudinal patterns of atrophy in clinical variants of frontotemporal lobar degeneration.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, p. 1, doi. 10.1002/alz.053807
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- Publication type:
- Article
New MAPT variant in a FTD patient with Alzheimer's disease phenotype at onset.
- Published in:
- 2021
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- Publication type:
- Letter
Emotional imagination of negative situations: Functional neuroimaging in anorexia and bulimia.
- Published in:
- PLoS ONE, 2021, v. 16, n. 4, p. 1, doi. 10.1371/journal.pone.0231684
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- Publication type:
- Article
Machine Learning Profiling of Alzheimer's Disease Patients Based on Current Cerebrospinal Fluid Markers and Iron Content in Biofluids.
- Published in:
- Frontiers in Aging Neuroscience, 2021, v. 13, p. N.PAG, doi. 10.3389/fnagi.2021.607858
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- Publication type:
- Article
Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA project.
- Published in:
- Neurological Sciences, 2020, v. 41, n. 8, p. 2193, doi. 10.1007/s10072-020-04306-8
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- Publication type:
- Article
Understanding the Pathophysiology of Cerebral Amyloid Angiopathy.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 10, p. 3435, doi. 10.3390/ijms21103435
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- Publication type:
- Article
Iatrogenic early onset cerebral amyloid angiopathy 30 years after cerebral trauma with neurosurgery: vascular amyloid deposits are made up of both Aβ40 and Aβ42.
- Published in:
- 2019
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- Publication type:
- Letter
Sporadic MM-1 Type Creutzfeldt-Jakob Disease With Hemiballic Presentation and No Cognitive Impairment Until Death: How New NCJDRSU Diagnostic Criteria May Allow Early Diagnosis.
- Published in:
- Frontiers in Neurology, 2018, p. 1, doi. 10.3389/fneur.2018.00739
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- Publication type:
- Article
Early Cognitive, Structural, and Microstructural Changes in Presymptomatic C9orf72 Carriers Younger Than 40 Years.
- Published in:
- JAMA Neurology, 2018, v. 75, n. 2, p. 236, doi. 10.1001/jamaneurol.2017.4266
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- Publication type:
- Article
The CSF neurofilament light signature in rapidly progressive neurodegenerative dementias.
- Published in:
- Alzheimer's Research & Therapy, 2018, v. 10, p. 1, doi. 10.1186/s13195-017-0331-1
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- Publication type:
- Article
Alzheimer neuropathology without frontotemporal lobar degeneration hallmarks ( TAR DNA-binding protein 43 inclusions) in missense progranulin mutation Cys139 Arg.
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- Brain Pathology, 2018, v. 28, n. 1, p. 72, doi. 10.1111/bpa.12480
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- Publication type:
- Article
Cognitive and Neurophysiological Effects of Non-invasive Brain Stimulation in Stroke Patients after Motor Rehabilitation.
- Published in:
- Frontiers in Behavioral Neuroscience, 2016, p. 1, doi. 10.3389/fnbeh.2016.00135
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- Publication type:
- Article
Brain correlates of alexithymia in eating disorders: A voxel-based morphometry study.
- Published in:
- Psychiatry & Clinical Neurosciences, 2015, v. 69, n. 11, p. 708, doi. 10.1111/pcn.12318
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- Publication type:
- Article
Neurofunctional Signature of Hyperfamiliarity for Unknown Faces.
- Published in:
- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0129970
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- Publication type:
- Article
Double-Cone Coil TMS Stimulation of the Medial Cortex Inhibits Central Pain Habituation.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0128765
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- Publication type:
- Article
Posterior Cortical Atrophy as an Extreme Phenotype of GRN Mutations.
- Published in:
- JAMA Neurology, 2015, v. 72, n. 2, p. 224, doi. 10.1001/jamaneurol.2014.3308
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- Publication type:
- Article
Extensive White Matter Involvement in Patients With Frontotemporal Lobar Degeneration Think Progranulin.
- Published in:
- JAMA Neurology, 2014, v. 71, n. 12, p. 1562, doi. 10.1001/jamaneurol.2014.1316
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- Publication type:
- Article
Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration.
- Published in:
- Neurogenetics, 2014, v. 15, n. 2, p. 95, doi. 10.1007/s10048-014-0389-x
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- Publication type:
- Article
DCTN1 Mutation Analysis in Families With Progressive Supranuclear Palsy-Like Phenotypes.
- Published in:
- JAMA Neurology, 2014, v. 71, n. 2, p. 208, doi. 10.1001/jamaneurol.2013.5100
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- Publication type:
- Article
NEUROANATOMICAL CORRELATES OF STATE OF MIND WITH RESPECT TO ATTACHMENT IN PATIENTS WITH ANOREXIA NERVOSA.
- Published in:
- Clinical Neuropsychiatry, 2013, v. 10, n. 5, p. 217
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- Publication type:
- Article
Brain metabolism changes after therapy with chenodeoxycholic acid in a case of cerebrotendinous xanthomatosis.
- Published in:
- 2013
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- Publication type:
- Letter
The Recognition of Facial Emotions in Spinocerebellar Ataxia Patients.
- Published in:
- Cerebellum, 2011, v. 10, n. 3, p. 600, doi. 10.1007/s12311-011-0276-z
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- Publication type:
- Article
Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patients.
- Published in:
- Brain Structure & Function, 2011, v. 216, n. 3, p. 275, doi. 10.1007/s00429-011-0310-4
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- Publication type:
- Article
A previously undiagnosed case of Gerstmann-Sträussler-Scheinker disease revealed by PRNP gene analysis in patients with adult-onset ataxia.
- Published in:
- 2008
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- Publication type:
- journal article
A previously undiagnosed case of Gerstmann-Sträussler-Scheinker disease revealed by PRNP gene analysis in patients with adult-onset ataxia.
- Published in:
- Movement Disorders, 2008, v. 23, n. 10, p. 1468, doi. 10.1002/mds.21953
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- Publication type:
- Article
Mutations in the POLG1 gene are not a relevant cause of cerebellar ataxia in Italy.
- Published in:
- Journal of Neurology, 2008, v. 255, n. 7, p. 1079, doi. 10.1007/s00415-008-0772-3
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- Publication type:
- Article